Canonical Allele Identifier: CA345392685

Gene: ACTN2

Linked Data

• MyVariant Identifiers: chr1:g.236925897T>G (hg19) ; chr1:g.236762597T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.236762597T>G , CM000663.2:g.236762597T>G	GRCh38
NC_000001.10:g.236925897T>G , CM000663.1:g.236925897T>G	GRCh37
NC_000001.9:g.234992520T>G	NCBI36
NG_009081.1:g.81128T>G
NG_009081.2:g.103457T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000542672.7:c.2663T>G	ENSP00000443495.1:p.Leu888Arg
ENST00000461367.2:n.959T>G
ENST00000492634.7:n.2593T>G
ENST00000682015.1:c.2570T>G	ENSP00000506961.1:p.Leu857Arg
ENST00000682490.1:n.581T>G
ENST00000682692.1:n.3758T>G
ENST00000682966.1:n.8304T>G
ENST00000683111.1:c.*1949T>G	ENSP00000507913.1:n.*1949T>G
ENST00000683322.1:n.4015T>G
ENST00000683805.1:n.1454T>G
ENST00000684050.1:n.5301T>G
ENST00000684122.1:n.2097T>G
ENST00000684286.1:n.4218T>G
ENST00000684502.1:n.3960T>G
ENST00000684763.1:n.1278T>G
ENST00000366578.6:c.2663T>G MANE Select	ENSP00000355537.4:p.Leu888Arg
ENST00000492634.6:n.2593T>G
ENST00000542672.6:c.2663T>G	ENSP00000443495.1:p.Leu888Arg
ENST00000651091.1:c.2353T>G	ENSP00000498677.1:n.2353T>G
ENST00000651275.1:c.2555T>G	ENSP00000498926.1:p.Leu852Arg
ENST00000651781.1:c.1743T>G
ENST00000651786.1:c.*2035T>G	ENSP00000498364.1:n.*2035T>G
ENST00000652096.1:c.*2068T>G	ENSP00000498896.1:n.*2068T>G
ENST00000366578.5:c.2663T>G	ENSP00000355537.4:p.Leu888Arg
ENST00000542672.5:c.2663T>G	ENSP00000443495.1:p.Leu888Arg
ENST00000546208.5:c.2039T>G	ENSP00000438384.2:p.Leu680Arg
NM_001103.3:c.2663T>G	NP_001094.1:p.Leu888Arg
NM_001278343.1:c.2663T>G	NP_001265272.1:p.Leu888Arg
NM_001278344.1:c.2039T>G	NP_001265273.1:p.Leu680Arg
NM_001278343.2:c.2663T>G	NP_001265272.1:p.Leu888Arg
NM_001103.4:c.2663T>G MANE Select	NP_001094.1:p.Leu888Arg
NM_001278344.2:c.2039T>G	NP_001265273.1:p.Leu680Arg